Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice

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Article

Reference

Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice

CHENNUPATI, Ramesh, et al.

Abstract

Endothelial arginase 1 was ablated to assess whether this prevents hyperglycemia-induced endothelial dysfunction by improving arginine availability for nitric oxide production.

Endothelial Arg1-deficient mice (Arg1-KOTie2 ) were generated by crossing Arg1fl/fl (controls) with Tie2Cretg/- mice and analyzed by immunohistochemistry, measurements of hemodynamics, and wire myography. Ablation was confirmed by immunohistochemistry.

Mean arterial blood pressure was similar in conscious male control and Arg1-KOTie2 mice.

Depletion of circulating arginine by intravenous infusion of arginase 1 or inhibition of nitric oxide synthase activity with L-NG -nitro-arginine methyl ester increased mean arterial pressure similarly in control (9 ± 2 and 34 ± 2 mmHg, respectively) and Arg1-KOTie2 mice (11 ± 3 and 38 ± 4 mmHg, respectively). Vasomotor responses were studied in isolated saphenous arteries of 12- and 34-week-old Arg1-KOTie2 and control animals by wire myography. Diabetes was induced in 10-week-old control and Arg1-KOTie2 mice with streptozotocin, and vasomotor responses were studied 10 weeks later. Optimal [...]

CHENNUPATI, Ramesh, et al . Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice. Physiological Reports , 2018, vol. 6, no. 11, p. e13717

DOI : 10.14814/phy2.13717 PMID : 29890043

Available at:

http://archive-ouverte.unige.ch/unige:107201

Disclaimer: layout of this document may differ from the published version.

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Deletion of endothelial arginase 1 does not improve vasomotor function in diabetic mice

Ramesh Chennupati^1,2,3,4, Merlijn J. Meens^2,5, Ben J. Janssen^2,3, Paul van Dijk¹,

Theodorus B. M. Hakvoort⁶, Wouter H. Lamers^1,4, Jo G. R. De Mey^2,3,7,8& S. Eleonore Koehler^1,4

1 Departments of Anatomy & Embryology, Maastricht University, Maastricht, the Netherlands 2 Department of Pharmacology & Toxicology, Maastricht University, Maastricht, the Netherlands 3 Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands

4 Nutrim - School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, the Netherlands 5 Department of Pathology and Immunology, University of Geneva, Geneva, Switzerland

6 Tytgat Institute for Liver & Intestinal Research, Academic Medical Center, Amsterdam, the Netherlands

7 Department of Cardiovascular and Renal Research, Institute of Molecular Medicine, University of Southern Denmark, Odense, Denmark 8 Department of Cardiac, Thoracic and Vascular Surgery, Odense University Hospital, Odense, Denmark

Keywords

Arginase 1 deficiency, endothelial dysfunction, nitric oxide.

Correspondence

S. Eleonore Koehler, Department of Anatomy& Embryology, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.

Tel: 0031 43388 1191 Fax: 0031 43388 4134

E-mail:leo.koehler@maastrichtuniversity.nl Funding Information

This work was supported by the grant from Dutch Heart Foundation (NHS) project 2008B107.

Received: 25 February 2018; Revised: 29 April 2018; Accepted: 30 April 2018 doi: 10.14814/phy2.13717 Physiol Rep, 6 (11), 2018, e13717, https://doi.org/10.14814/phy2.13717

Abstract

Endothelial arginase 1 was ablated to assess whether this prevents hyperglycemia-induced endothelial dysfunction by improving arginine availability for nitric oxide production. Endothelial Arg1-deficient mice (Arg1-KO^Tie2) were generated by crossing Arg1^fl/fl(controls) with Tie2Cre^tg/ mice and analyzed by immunohistochemistry, measurements of hemodynamics, and wire myography. Ablation was confirmed by immunohistochemistry. Mean arterial blood pressure was similar in conscious male control and Arg1-KO^Tie2 mice.

Depletion of circulating arginine by intravenous infusion of arginase 1 or inhibition of nitric oxide synthase activity with L-N^G-nitro-arginine methyl ester increased mean arterial pressure similarly in control (92 and 342 mmHg, respectively) and Arg1-KO^Tie2 mice (113 and 384 mmHg, respectively). Vasomotor responses were studied in isolated saphenous arteries of 12- and 34-week-old Arg1-KO^Tie2 and control animals by wire myography. Diabetes was induced in 10-week-old control and Arg1- KO^Tie2 mice with streptozotocin, and vasomotor responses were studied 10 weeks later. Optimal arterial diameter, contractile responses to phenylephrine, and relaxing responses to acetylcholine and sodium nitroprusside were similar in normoglycemic control and Arg1-KO^Tie2 mice. The relaxing response to acetylcholine was dependent on the availability of extracellular ^L- arginine. In the diabetic mice, arterial relaxation responses to endothelium- dependent hyperpolarization and to exogenous nitric oxide were impaired.

The data show that endothelial ablation of arginase 1 in mice does not markedly modify smooth muscle and endothelial functions of a resistance artery under normo- and hyperglycemic conditions.

Introduction

Vascular complications are the primary cause of morbid- ity and mortality in diabetics. Endothelial dysfunction is considered a critical factor in the development of these complications (Luscher et al. 2003; Sena et al. 2013). One aspect of endothelial dysfunction is a decrease in the bioavailability of endothelium-derived nitric oxide

(EDNO). This decrease may be caused by lowered endothelial nitric oxide synthase (NOS3) activity, increased levels of endogenous NOS inhibitors, limited availability of the NOS3 substrate arginine (Luscher et al.

2003; Cooke et al. 1991; Wu and Meininger 2000), or increased scavenging of nitric oxide (NO) by reactive oxygen species (ROS) (Gryglewski et al. 1986). Under healthy, physiological conditions, sufficient L-arginine is

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available for NO production in the endothelium. How- ever, this may be altered in pathological conditions, such as diabetes, where arginine availability for NO synthesis may be becoming limited. We previously showed that under diabetic conditions arginine resynthesis from citrulline is necessary to maintain arginine supply for NO- mediated arterial relaxation (Chennupati et al. 2014).

Arginine-resynthesizing enzymes (i.e., the enzymes of the citrulline-NO cycle) and arginine-catabolizing enzymes (arginases, ARG) tightly regulate intracellular arginine concentrations (Li et al. 2001). The two arginase isoforms, ARG1 and ARG2, have similar kinetic proper- ties, but are encoded by separate genes. Both ARG1 and ARG2 proteins were demonstrated in endothelium (for a review, see Pernow and Jung (2013)) and implicated in endothelial dysfunction. IncreasedArg1expression is associated with endothelial dysfunction in diabetic patients (Bagi et al. 2013; Beleznai et al. 2011) and mice (Romero et al. 2012; Toque et al. 2013a).

To evaluate roles of arginases, three constitutive knockout mouse models were previously developed:

Arg1 ^/ (Iyer et al. 2002), Arg2 ^/ (Shi et al. 2001), and double knockout (KO) mice (Deignan et al. 2006).

Arg ^/ and double KO mice develop severe hyperam- monemia and die within 10–14 days after birth (Iyer et al. 2002). Intriguingly, heterozygous, constitutive partial ablation of ARG1 (Arg1^+/ ), complete deletion of ARG2 (Arg2 ^/ ), and the combination of these two genotypes (Arg1^+/ /Arg2 ^/ ) partially rescue diabetes- induced, endothelial dysfunction in mouse aorta and corpus cavernosum (Romero et al. 2012; Toque et al.

2011). Because Arg1 ^/ mice do not survive beyond 2 weeks after birth, the role of ARG1 in vascular dysfunction has not been investigated. We hypothesized that limitation of the capacity of the endothelium to degrade arginine via ARG1 improves arterial endothelium-dependent relaxation, especially when NO-mediated relaxations are compromised (as in diabetic mice). This question is pertinent because ARG1 and NOS3 compete for the same substrate. We tested this hypothesis in saphenous arteries of normoglycemic and diabetic mice that did or did not express ARG1 in their endothelium, because these muscular resistance arteries are sensitive to impair- ment of the NO-citrulline cycle (Chennupati et al.

2014).

Materials and Methods

Animals

All procedures were approved by the Committee for Ani- mal Care and Use of Maastricht University (DEC 2008- 182 and 2012-027) and performed in accordance with

their guidelines. Endothelial ablation of ARG1 was achieved by crossingArg1^fl/fl(Cloots et al. 2013) andTie2- Cre^tg/ (Kisanuki et al. 2001) mice. Mice that lack ARG1 in their endothelium (Arg1^fl/fl/Tie2Cre^tg/ ) are named Arg1-KO^Tie2 hereafter. We have previously shown that mice carrying the fully functional floxed alleles of the ARG1 gene (Arg1^fl/fl) are indistinguishable from their wild-type littermates (Cloots et al. 2013). Therefore,

Arg1^fl/fl/Tie2Cre ^/ littermates were used as control ani-

mals; 12- and 34-week-old male and female mice were used. Mice were housed in standard cages (constant room temperature and humidity, 12 h light/dark cycles) and had free access to standard pelleted chow and tap water.

Diabetes was induced at the age of 10 weeks by intraperitoneal (IP) injections of streptozotocin (STZ;

50 mgkg ¹) on 5 consecutive days (American diabetes complications consortium AMDCC protocols; https://

www.diacomp.org). Blood glucose was measured following overnight fasting at 1, 4, and 10 weeks following STZ injections (Table S5), and male mice with stable blood glucose concentration of≥20 mmolL ¹were used for the

experiments (meanSEM: controls

22.80.8 mmolL ¹, n =10 (Chennupati et al. 2014);

Arg1-KO^Tie2 23.10.6 mmolL ¹, n =5). Female mice were not included in the experiments because their fasting blood glucose concentrations only transiently increased to

~60% of the values measured in males at 1 and 4 weeks after STZ treatment and returned to pretreatment values between 4 and 10 weeks (mean SEM at 10 weeks: controls 7.81.0 mmolL ¹, n =8; Arg1-KO^Tie2 7.60.9 mmolL ¹, n =4; Table S5; cf Chennupati et al. 2014). This finding suggests that the b cells of female mice are more resistant to STZ and regenerate between 4 and 10 weeks after the treatment.

Solutions and drugs

Krebs-Ringer bicarbonate-buffered salt solution (KRB) contained (in mmolL ¹): 118.5 NaCl, 4.7 KCl, 2.5 CaCl2, 1.2 MgSO4, 1.2 KH2PO4, 25.0 NaHCO3, and 5.5 glucose.

The KRB solution was continuously aerated with 95%

O2/5% CO2 and maintained at 37°C. Indomethacin (INDO; Sigma Aldrich, Zwijndrecht, NL) was dissolved in ethanol. Acetylcholine (ACh), noradrenaline (NA), phenylephrine (PHE), N^x-nitro-arginine methyl ester (L- NAME), and sodium nitroprusside (SNP; all Sigma Aldrich) were dissolved in KRB solution. High K⁺-KRB solution was prepared by replacing 40 mmolL ¹ NaCl with KCl. Buffers containing intermediate K⁺ concentrations were prepared by mixing KRB and K⁺-KRB. In the

L-arginine-depletion experiment (Fig. 4), KRB was replaced by ^L-arginine-free Iscove’s modified Dulbecco’s medium.

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Plasma amino acid analysis

To determine plasma amino acids, blood was drawn from the inferior vena cava using a heparinized syringe, cen- trifuged, deproteinized by adding 50lL plasma to tubes containing 4 mg sulfosalicylic acid, and stored at 80°C.

Amino acid concentrations were determined by HPLC (van Eijk et al. 1993).

Immunohistochemistry

Saphenous arteries were fixed in formaldehyde (4%) or cold acetone/methanol/water (2:2:1; 4°C) overnight, dehy- drated, and embedded in paraffin. Sections (4lm) were incubated overnight at 4°C with rabbit antibodies direc- ted against ARG1 (1:10,000 in 10% normal goat serum NGS; AMC, Amsterdam; de Jonge et al. 2002). Antibody binding was visualized with alkaline phosphatase (AP)- coupled goat anti-rabbit IgG antibodies (diluted 1:200 in Teng-T/10% NGS: 100 mmolL ¹ Tris-HCl, pH 8.0, 50 mmolL ¹ EDTA, 1.5 mmolL ¹ NaCl, 2.5% (w/v) gelatin, 0.5% (v/v) Tween 20, 10% (v/v) NGS) and incubation with AP substrate (NBT/BCIP) for 15–90 min at room temperature. Negative controls were incubated with secondary antibody only. Background staining was equalized by globally adapting the brightness of colors with Adobe Photoshop, with panels C and G serving as reference. The contrast was modified in the H&E-stained panels E and H only.

Determination and manipulation of hemodynamic parameters

We determined hemodynamic parameters in conscious, unrestrained control, and Arg1-KO^Tie2 mice. Heparinized indwelling polyethylene catheters were introduced into the femoral artery and jugular vein under isoflurane anes- thesia 2 days before the experiments (Janssen et al. 2000).

Analgesia was obtained by perioperative subcutaneous injections of buprenorphine (0.03 mgkg ¹). On the day of the experiment, the arterial line was connected to a pressure transducer (Micro Switch 150 PC) and the signal was sampled at 2.5 kHz. Mean arterial pressure (MAP) and heart rate (HR) were derived from this signal using the IDEEQ data acquisition system (Instrument Services, Maastricht University, NL). The venous line was extended outside the cage and filled with a 0.9% NaCl solution.

Hemodynamic parameters were allowed to stabilize before pharmacological interventions. The following compounds were applied via an intravenous catheter: 200 U purified bovine ARG1 (Cell Sciences, Canton, MA, USA) dissolved in 125 lL HEPES buffer (pH 7.4) or L-NAME (10 mgkg ¹) dissolved in 0.9% saline. After the

experiments, animals were euthanized with 250 mgkg ¹ pentobarbital administered through the catheter. Cannu- lation of femoral arteries in diabetic mice is associated with a full occlusion of the main feeding artery of the leg.

In those mice, wound healing and revascularization are so much impaired that the leg becomes necrotic. For this reason, diabetic mice could not be subjected to the same protocol as the nondiabetic mice.

Organ chamber experiments

Animals were euthanized by CO2/O2 inhalation. Saphe- nous arteries were dissected free from perivascular adi- pose tissue and mounted in a wire myograph (Danish Myotechnology, Aarhus, DK). Arterial segments (2 mm) were distended to the diameter at which maximal contractile responses to 10lmolL ¹ NA were obtained (Chennupati et al. 2013; Hilgers et al. 2010). Optimal diameters (Dopt) and maximal contractile responses to NA are summarized in Table S2.

Contributions of NO, endothelium- dependent hyperpolarization (EDH) and cyclooxygenase products to endothelium- dependent relaxation

Initially, a concentration-response curve (CRC) for PHE (0.01–10lmolL ¹) was recorded. Following the contraction induced by 10 lmolL ¹ PHE, an ACh CRC (0.01–

10lmolL ¹) was generated. Next, arteries were contracted using K⁺(40 mmolL ¹), and again an ACh CRC (0.01–10lmolL ¹) was recorded. These experiments were repeated in the presence of the cyclooxygenase inhibitor INDO (10lmolL ¹) and in the presence of both INDO and the NOS inhibitor L-NAME (100 lmolL ¹) to assess the contribution of NO to arterial relaxation (Morikawa et al. 2005; Matoba et al. 2000).

Sensitivity of vascular smooth muscle to NO During contraction of the saphenous arteries with PHE (10lmolL ¹) in the presence of INDO (10 lmolL ¹) and L-NAME (100 lmolL ¹), the relaxing effects of the NO-donor SNP (0.01–10lmolL ¹) were recorded.

Statistical analysis

All CRCs for contractile stimuli are expressed as percentage of the maximal response to 10lmolL ¹ NA prior to the administration of pharmacological inhibitors. Relaxing responses were expressed as percentage reduction of the level of contraction. Individual CRCs were fitted to a non- linear sigmoid regression curve (Graphpad Prism 5.0).

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Sensitivity, maximal effect (Maximal response), and amino acid concentrations are shown as meansSEM. Two-way ANOVA followed by a Bonferroni post hoc test was used to compare multiple groups. Group statistics for hemodynamic parameters were analyzed by an independent sam- ples test to determine differences between genotypes, followed by pairedt-tests to assess the effects of treatments.

Results

Ablation of ARG1 protein from endothelial cells

Endothelial ablation of ARG1 was achieved by crossing

Arg1^fl/fl and Tie2Cre^tg/ mice. Mice that lack ARG1 in

their endothelium (Arg1^fl/fl/Tie2Cre^tg/ ) are named Arg1- KO^Tie2 hereafter. We have previously shown that mice carrying the fully functional floxed alleles of the ARG1 gene (Arg1^fl/fl) are indistinguishable from their wild-type littermates (Cloots et al. 2013). Therefore, Arg1^fl/fl/ Tie2Cre ^/ littermates were used as control animals. To verify endothelial deletion of ARG1 protein, saphenous artery sections were stained for ARG1. The sensitivity of immunohistochemical staining for ARG1 in endothelial cells was much improved by fixation of the tissues in acetone/methanol/water (2:2:1) instead of formaldehyde. In young adult control mice, endothelial ARG1 was weakly expressed (Fig. 1A and E). In line with earlier observa- tions (Romero et al. 2012; Toque et al. 2013a; White et al. 2006; Pernow et al. 2015), we observed stronger expression of ARG1 in arteries of 34-week-old control (Fig. 1B and F) and 22-week-old diabetic mice (Fig. 1C and G), but not in diabetic Arg1-KO^Tie2 mice (Fig. 1D and H). Specificity of the antibody-staining procedure was demonstrated by zonated ARG1 expression in liver sections (Fig. S1) (Dingemanse et al. 1996).

Plasma amino acid concentrations in control and Arg1-KO^Tie2mice

Especially in diabetes, upregulation of arginase expression can limit the availability of arginine for NOS in aging vessels (Romero et al. 2012; Toque et al. 2013a; Pernow et al. 2015; Santhanam et al. 2008). Thus, absence of endothelial ARG1 might improve endothelial function by increasing arginine availability for NOS3 in diabetic mice.

We only studied male diabetic mice, because the AMDCC protocol induced only transient hyperglycemia in female C57BL/6 mice (see M&M section). Plasma arginine concentrations were similar in control and Arg1-KO^Tie2mice (Tables 1 and S1). Despite increased ARG1 expression in the endothelium of diabetic control mice, their plasma arginine concentration was comparable to that of

normoglycemic control mice. In diabetic Arg1-KO^Tie2 mice, however, the plasma arginine concentration was increased (~30%; P= 0.030). The concentration of the arginine precursor citrulline was increased in diabetic mice compared with normoglycemic mice, while that of tryptophan was significantly decreased in diabetic Arg1- KO^Tie2 mice, and a trend (P=0.054) toward a decrease was observed in diabetic control mice (Tables 1 and S1).

Hemodynamic parameters in male control and Arg1-KO^Tie2mice

To assess the effects of endothelial Arg1 ablation on hemodynamics, mean arterial pressure (MAP) and heart rate (HR) were recorded in conscious male mice. Basal MAP did not differ between conscious unrestrained control and Arg1-KO^Tie2 mice (P=0.777). MAP after arginase infusion did not differ between control and Arg1- KO^Tie2 mice (P=0.257), demonstrating that endothelial Arg1ablation does not influence the hemodynamic effects of circulating arginine. Accordingly, data from both groups were pooled. The effects of circulating arginine on blood pressure maintenance were assessed by a bolus injection of 200U ARG1, which rapidly decreases the concentration of circulating arginine to~13% of the original plasma concentration during at least 20 min (Chennupati et al. 2014; Wijnands et al. 2015). This intervention resulted in a small but significant rise of MAP to 108% of control values (92.5 mmHg increase, P=0.007;

Fig. 2). Again, control and Arg1-KO^Tie2mice did not differ significantly (P=0.115). To compare the effects of arginine depletion to those of NOS inhibition, the same animals received a bolus injection of the NOS inhibitor L-NAME (10 mgkg ¹) 24 h later. This treatment resulted in a 362 mmHg increase in MAP (P<0.000), that is, in a fourfold higher increase than that caused by plasma arginine depletion. No significant differences were observed between knockout and wild-type animals.

Basal HR did not differ between control (65121 beats/min, n =6) and Arg1-KO^Tie2 mice (71342 beats/min, n =6, P=0.186, Table 2). The decrease in circulating arginine concentration upon injection of 200U ARG1 (previous paragraph) had no significant effect on HR and again, and no difference between genotypes was observed. Accordingly, data of control and Arg1- KO^Tie2animals were pooled (Table 2). HR decreased to a similar extent in L-NAME-treated control and Arg1-KO^Tie2 mice ( 18946/min,n =7,P=0.006).

Reactivity of isolated saphenous arteries Endothelial ARG1 deficiency might entail compensatory mechanisms such as increased arterial contractility or

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decreased vasodilator responses to maintain blood pressure. We, therefore, studied the effects of endothelial Arg1 ablation on vasomotor responses in more detail in saphenous arteries isolated from male and female mice of 12- and 34-week-old control and Arg1-KO^Tie2 mice, and 22-week-old male STZ-treated mice of both genotypes.

Contractile responses of control and Arg1-KO^Tie2 arteries

The maximal contractile response to 10 lmolL ¹ noradrenaline (NA) was comparable in 12- and 34-week- old male and female control and Arg1-KO^Tie2 mice (Tables S2 (male); S5 (female mice). The sensitivity and maximal contractile response to phenylephrine (PHE) (0.01–10lmolL ¹) or K⁺ (40 mmolL ¹) in the absence and presence of L-NAME (100 lmolL^-1) or indomethacin (cyclooxygenase inhibitor, INDO;

10lmolL^-1) and a combination of the former did also not differ significantly between groups (Tables S2, S5).

Contractile responses did not differ significantly between saphenous arteries from male diabetic Arg1- KO^Tie2 and control mice (Table S2), showing that a decreased capacity for endothelial arginine degradation does not improve contractile responses of vessels in diabetic mice.

Acetylcholine (ACh)-induced relaxations during PHE-induced contractions

ACh-induced relaxations were studied during PHE- induced contractions. In the absence of pharmacological inhibitors and in the presence of INDO, the maximal response and sensitivity to ACh were similar in control and Arg1-KO^Tie2mice of both sexes and both age groups (Fig. 3A and D male mice and S2 female mice, Tables 3, S3, S4, S5). INDO had no statistically significant effects on ACh-relaxation irrespective of genotype or age (Fig. 3A, B, D and E). The combination of INDO and L- LAME reduced ACh-induced relaxations to a similar degree in all groups of nondiabetic arteries (Fig. 3B, C, E and F). Thus, in control arteries, the presence or absence of endothelial ARG1 does not affect endothelium-dependent relaxation. As shown earlier in mesenteric arteries (Morikawa et al. 2005), diabetes reduced the relaxation responses in saphenous arteries (Fig. 3G, H and I). How- ever, the maximal response and sensitivity of ACh- induced relaxations did not differ between diabetic control and diabetic Arg1-KO^Tie2 mice in any of conditions tested (Fig. 3G, H and I).

In view of the above-described lack of an effect of genotype on ACh-induced arterial relaxations, we studied whether the extracellular ^L-arginine concentration can be

A B C D

E F G H

Figure 1. Expression of ARG1 protein in saphenous arteries of male mice. Panel (A): control, panel (B): 8-month-old normoglycemic control, panel (C): diabetic control (DM), panel (D): diabetic Arg1-KO^Tie2mice. Panels (E, F, G) and (H) show the complementary H&E staining of a serial section of the respective arteries. Arrows indicate endothelial cells. All tissues were fixed with acetone/methanol/water (see Materials and Methods).

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limiting for these relaxations in control mice. We, therefore, subjected isolated arteries in L-Arg-free Iscove’s modified Dulbecco’s medium to 14 consecutive contraction-relaxation cycles at 20-min intervals. Figure 4A shows that the sensitivity and maximal response to ACh progressively decreased. To demonstrate that this was due to ^L-arginine depletion, we repeated the experiment and added ^L-arginine to the culture medium after the last contraction-relaxation cycle (Fig. 4B). Partial restoration of the relaxing response to ACh demonstrates that the decline of the relaxing response indeed resulted from L- Arg depletion.

Endothelium-derived NO

Endothelium-derived NO (EDNO) contributes to endothelium-dependent relaxation of muscular resistance arteries (Chennupati et al. 2013). To test for differences in EDNO release, we inhibited endothelium-dependent hyperpolarization (EDH) by depolarizing the vessels with high potassium buffer (40 mmolL ¹K⁺) and by inhibit- ing cyclooxygenases using INDO (Chennupati et al.

2013). Under these conditions, relaxing responses to ACh can entirely be attributed to NO (Chennupati et al.

Table 1. Effect ofArg1ablation on plasma amino acid concentrations in 12-week-old healthy male and 22-week-old male diabetic mice.

Plasma amino acids [lmolL] Control Arg1-KO^Tie2 Control STZ-treated Arg1-KO^Tie2STZ-treated

Alanine 48425 39072 50051 57567

Arginine 10313 12626 1219 1568¹

Asparagine 4615 3311 395 6113

Ornithine 914 798 1009 11615

Citrulline 525 464 785² 857²

Glutamic acid 889 8015 9710 11014

Glutamine 51880 518102 53729 57755

Glycine 27616 26035 23613 27526

Histidine 715 615 565 594

Isoleucine 9710 878 17021 19242

Leucine 15911 15414 27936 31368

Lysine 25620 25632 33667 48578

Methionine 431 404 374 485

Phenylalanine 4310 595 593 727

Taurine 7211 7312 806 13115^2,1

Serine 13216 11517 12911 14921

Threonine 13217 11615 14013 16921

Tryptophan 25921 25533 16919 15916²

Tyrosine 33231 40443 31238 30627

Valine 25915 22013 38749 43290

ΣAA 3578256 3449407 3863215 4851554

Arginine-availability index 0.330.03 0.320.02 0.360.05 0.260.03

All values are shown as meansSEM.

1P<0.05 compared with the corresponding control group (knockout vs. wild type).

2P<0.05 compared with the corresponding healthy group (diabetes vs. healthy). Control:n=3; Arg1-KO^Tie2: n=4; STZ-control: n=14;

STZ-Arg1-KO^Tie2:n=6. Arginine-availability index: [Arg]/([Orn]+[Lys]). ForP-values of the comparisons, see Table S1.

Figure 2. Effects of endothelialArg1ablation on mean arterial blood pressure (MAP) in 34-week-old conscious male mice. Blood pressure was measured in the same mice 2 (Basal,+Arginase) and 3 days (Basal 2,+L-NAME) after implantation of a femoral artery catheter connected to a pressure transducer. Since MAP in control and Arg1-KO^Tie2mice did not differ either under basal or treatment conditions, data from both groups were pooled. Left side: MAP under basal conditions and after a bolus injection of 200U bovine ARG1 via a jugular vein catheter. Right side: MAP under basal conditions one day later (Basal 2) and after intravenous L-NAME (10 mgkg ¹) injection (right). Values are meansSEM. Nine mice (five control+four Arg1-KO^Tie2) received the arginase infusion; due to loss of catheter patency in one control mouse, eight mice received the L-NAME infusion. Differences between treatments were analyzed with a pairedt-test.

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Table 2. Effects of genotype, arginase 1, and L-NAME treatment on heart rate in conscious male mice.

Comparison of genotypes Effect of treatment

Control [beats. min ¹] ARG1-KO^Tie2[beats. min ¹] P DHR [bp. min ¹] P

Basal HR 65121 71342 0.184

Before ARG1 65737 73345 0.230 ARG1 3933 0.276

After ARG1 62735 69349 0.326

Before L-Name 66130 76848 0.109 L-NAME 18946 0.006

After L-NAME 52515 53166 0.914

Heart rate was determined as described in Materials and Methods. Values are given as meansSEM. Differences between genotypes were assessed with an independentt-test (nper group 3–5 animals). Since control and Arg1-KO^Tie2mice did not differ significantly under any of the conditions tested, all animals were pooled to assess the effect of the treatments with a pairedt-test (nfor ARG1=9, L-NAME=7).

Figure 3. Effects of endothelialArg1ablation on relaxation responses to ACh (0.01–10lmolL ¹) during PHE- (10lmolL ¹) induced contractions in saphenous arteries isolated from 12- (panels A–C) or 34- (panels D–F) week-old normoglycemic and 22-week-old hyperglycemic (panels G–I) male mice. Black squares: control mice; white circles: Arg1-KO^Tie2mice. Panels (A, D, G) in the absence of pharmacological inhibitors. Panels (B, E, H) in the presence of indomethacin (INDO, 10lmol.L ¹). Panels (C, F, I) in the presence of INDO (10lmolL ¹) and L- NAME (100lmolL ¹). Values are shown as meansSEM (n=5–7; for the number of animals per individual experiment, see Table S2).

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2013). These responses were comparable in all groups of mice (Fig. S2; Tables 3 and S3).

Relaxing responses to SNP

To study that the genetic modification did not affect responses of vascular smooth muscle cells to exogenous

NO relaxations in response to the NO-donor sodium nitroprusside (SNP; 0.01–10lmolL ¹) were studied during PHE-induced contractions in the presence of INDO and L-NAME. Sensitivity and maximal response to SNP were comparable between control and Arg1-KO^Tie2 mice of both age groups and sexes (Fig. 5, Tables 3, S3 and S4). However, hyperglycemia resulted in a reduced

Table 3. Effect of endothelial ablation ofArg1on relaxation responses.

Control Arg1-KO^Tie2

Sensitivity Maximal response% n Sensitivity Maximal response% n

12-week-old mice

Without inhibitors 6.70.1 942 7 6.70.1 973 4

INDO 6.50.2 941 6 6.60.1 884 5

INDO+L-NAME 6.00.1 567 7 6.20.2 5712 5

Relaxation to EDNO 6.10.1 604 6 5.90.1 566 4

Relaxation to SNP 7.60.1 971 5 7.70.1 971 5

34-week-old mice

INDO 6.60.1 883 8 6.70.3 896 4

INDO+L-NAME NA 396 7 NA 298 4

Relaxation to SNP 7.50.1 971 7 7.60.3 981 5

22-week-old diabetic mice

INDO 6.50.1 814 8 6.50.2 767 5

INDO+L-NAME NA 185 7 NA 196 5

Relaxation to SNP 7.00.1² 981 7 6.80.1¹,² 961 5

Relaxation responses to acetylcholine (ACh; 0.01–10lmolL ¹) in PHE- (10lmolL ¹) or K⁺(40 mmolL ¹) contracted vessels were determined in the presence or absence of indomethacin (INDO, 10lmolL ¹) and L-NAME (100lmolL ¹). Maximal relaxation (Maximal response) is expressed as % reduction of the maximal contractile response to PHE (10lmolL ¹), except for endothelium-derived nitric oxide (EDNO) responses (% reduction of maximal contractile response to 40 mmolL ¹K⁺). In the presence of NOS inhibitor L-NAME (100lmolL ¹) and INDO (10lmolL ¹), the maximal relaxation to an NO-donor is determined by exposing the vessels to SNP (0.01–10lmolL ¹).

1P<0.05 compared with the corresponding control group (knockout vs. wild type).

2P<0.05 compared with the corresponding control group (diabetes vs. control). All values are shown as meanSEM.

Figure 4. The effect of 14 consecutive contraction-relaxation cycles (CRC) on ACh-induced relaxation during contractions induced by PHE (10lmolL ¹). Two-mm arterial segments were kept in L-Arg-free culture medium during the experiment. The EC50increased, whereas the Maximal response decreased with increasing number of CRCs (panel A). In a separate experiment (panel B), the arterial segments were subjected to repeated CRCs in L-Arg-free culture medium until relaxation had decreased to~25%. L-Arg (1 mmolL ¹) was then added. ACh- induced relaxations were tested after 60 min. CRC: contraction-relaxation cycle.

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sensitivity (sensitivity: 7.0 0.1) to SNP compared with 12- and 34-week-old normoglycemic control mice (sensitivity: 7.6 0.1 and 7.50.1, respectively; Fig. 5, Tables 2 and S3), as was described earlier (Csanyi et al.

2007). Ablation of endothelial arginase 1 (Arg1-KO^Tie2) further reduced arterial smooth muscle sensitivity to SNP (P=0.045; Fig. 5C, Tables 3 and S3).

Discussion

In this study, we tested the hypothesis that endothelial ablation of the Arg1 gene increases endothelium-dependent vasodilatation in muscular resistance arteries of control and diabetic mice. The major findings of this study are that (1) diabetic Arg1-KO^Tie2mice have a higher arginine concentration in plasma, (2) hemodynamics are not affected by endothelial ARG1 ablation, (3) vasomotor function is not affected by endothelial ARG1 deficiency in normoglycemic mice, and (4) diabetes-induced alterations in arterial smooth muscle reactivity and endothelium- dependent relaxations are not prevented by endothelial ARG1 ablation.

In this study, we used theTie2-Cre transgene (Kisanuki et al. 2001) to eliminate floxedArg1from the endothelium.

This transgene has an excellent reputation in eliminating floxed DNA sequences (Kisanuki et al. 2001, 2010; Hamada et al. 2005; Koni et al. 2001; Schlaeger et al. 2005) and, accordingly, was also effective in eliminating floxed Ass from the endothelium of the saphenous arteries in C57BL/6 mice (Chennupati et al. 2014). That study showed that resynthesis of arginine from citrulline was necessary to provide sufficient arginine for NO synthesis in saphenous arteries of diabetic mice (Chennupati et al. 2014). Further- more, we showed earlier that lipopolysaccharide-treated

Arg1-KO^Tie2mice produced more NO in the endothelium of their carotid arteries and jejunum than control mice (Wijnands et al. 2014). In addition, Arg1-KO^Tie2mice suffering from allergic asthma did not express ARG1 mRNA or protein in their lungs, even though this condition upregulates Arg1 expression >200-fold in control mice (Cloots et al. 2013). These data underscore our claim that Arg1 expression was eliminated from the endothelium.

TheTie2-Cre transgene is best known for its expression in cells of hematopoietic origin, such as endothelial cells and macrophages (Tang et al. 2010). Thus, in our Arg1- KO^Tie2mice, cells derived from the hematopoietic lineage are also devoid of ARG1, and this may have effects on circulating concentrations of citrulline and arginine.

Therefore, a contribution of Arg1 elimination in macrophages and/or erythrocytes to blood pressure responses cannot be ruled out. In fact, in a previous study with these mice, we observed effects of Arg1 ablation that could be attributed to either macrophages (cytokine production) or endothelium (NOS-dependent effects on the mucosal perfusion of villi in the jejunum) (Wijnands et al. 2014). However, it is highly unlikely that substantial numbers of erythrocytes and macrophages were present in the walls of the vessels used in the wire-myograph measurements. Ablation of Arg1 in cells of the myeloid lineage has been shown to increase TH2-mediated inflam- matory responses in mouse models of schistosoma infec- tion (Pesce et al. 2009). It is, therefore, possible that potential beneficial effects of endothelial Arg1 ablation are masked by increased vascular inflammation due to Arg1 ablation in cells of the myeloid lineage in those same mice, even though we did not find histological evidence of increased vascular inflammation in the vessel walls and

Figure 5. The effect of endothelialArg1ablation on relaxation responses to sodium nitroprusside (SNP, 0.01–10lmolL ¹) during PHE- (10lmolL ¹) induced contraction in saphenous arteries of 12- (panel A), 34- (panel B) week-old normoglycemic and 22-week-old diabetic (panel C) male mice. Black squares: control mice; white circles: Arg1-KO^Tie2. All experiments were performed in the presence of INDO (10lmolL ¹) and L-NAME (100lmolL ¹). Values are shown as meansSEM (n=5–7; for the number of animals per individual experiment, see Table S2).

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surrounding tissue. In a model of allergic asthma in the same mouse strain, we did not find an effect of Arg1 ablation on pulmonary inflammation as determined by cytokine expression and histology (Cloots et al. 2013).

We did, however, not investigate cytokine profiles, NO production or leukocyte adhesion to vessel walls in the current model and can, therefore, not exclude that some vascular inflammation was present that could have masked potential beneficial effects of endothelial Arg1 ablation.

A limitation of our genetic approach to eliminate Arg1 expression is that it may not be possible to selectively manipulate endothelial arginine concentrations in resistance arteries. In many vascular beds, resistance arteries exhibit heterocellular myoendothelial gap junctions (Dora et al. 2003; Sandow et al. 2012; Hilgers and De Mey 2009) through which arginine could diffuse from the smooth muscle to the endothelial cells and vice versa.

Arginine diffusion through these pores may compensate for changes in endothelial arginine concentration elicited by, for example, decreased arginine degradation in endothelial cells. In endothelial cells, gap junctions are primarily formed of the connexin proteins CX37 (GJA4), CX40 (GJA5) and CX43 (GJA1) (Meens et al. 2015).

Because the diabetic condition reduces their expression in vascular walls (Bobbie et al. 2010; Hou et al. 2008), reduced gap-junction activity could explain limited repletion of arginine in this condition (Chennupati et al.

2014). This hypothesis implies that the myoendothelial gap junction-dependent repletion of endothelial arginine is not sufficiently reduced to limit NOS activity irrespective of whether or not ARG1 is present in the endothelium. Unfortunately, this hypothesis is difficult to test, since inhibitors of gap-junction activity are well known to be nonselective (Matchkov et al. 2004). The alternative genetic approach is also complex, since it would require the production of an endothelium-specific triple knockout of C937, C9 40, and C943.

Both ARG1 and ARG2 are found in endothelium (Per- now and Jung 2013) and have been implicated in endothelial dysfunction. Toque et al. (Toque et al. 2013b) attributed a larger role to ARG1 than ARG2 in mediating hypertension. ARG1 also appears involved in diabetes as underscored in our study by the increased endothelial ARG1 staining in diabetic control mice and increased plasma arginine concentration in diabetic Arg1-KO^Tie2 mice.

One would assume that elimination of ARG1 should increase the circulating arginine concentration. However, in this study, such increase was only observed in diabetic Arg1-KO^Tie2 mice. The similar 30% increase in the summed concentration of amino acids suggests that the effect is not specific for arginine. In agreement, the

arginine-availability index (plasma [Arg]/([Orn]+[Lys])) did not change (Table 1). This index is a marker for the competitive strength of arginine over other basic amino acids for transport into endothelial cells (Morris et al.

2004). When plasma arginine was depleted acutely by ARG1 bolus injection, the arginine-availability index dropped to ~25% of the original (Wijnands et al. 2015).

In the present study, a similar intervention caused blood pressure to increase (Fig. 3A), implying that extracellular arginine availability had become limiting for blood pressure maintenance. However, even during this challenge, the increase in blood pressure was only ~30% of that achieved by inhibition of NOS by L-NAME, implying an important role for intra-endothelial arginine repletion or resynthesis by argininosuccinate synthase (ASS). This conclusion is underscored by our earlier findings in diabetic Ass-KO^Tie2 mice; the summed amino acid concentrations and the arginine-availability index were similar to controls (Chennupati et al. 2014) as in this study. Whereas no endothelial dysfunction developed in control Ass- KO^Tie2 mice, it did in diabetic Ass-KO^Tie2 mice, showing that the contribution of resynthesis of arginine via ASS to NO synthesis became a limiting factor in diabetes (Chennupati et al. 2014). In the jejunum of untreated Arg1-KO^Tie2 mice, on the other hand, NOS3 was hypo- phosphorylated on Thr495 and tended to be hyper-phosphorylated on Ser1177 (Wijnands et al. 2014), suggesting that Arg1 deficiency indeed increased NOS3 activity (Chen et al. 2008; Lin et al. 2003). In fact, we based our hypothesis that a limitation of the capacity of the endothelium to degrade arginine via ARG1 would improve arterial endothelium-dependent relaxation. The combination of our earlier finding that the diabetic condition does limit the ASS-mediated repletion of arginine and finding in the present study that endothelial Arg1 elimination does not improve direct smooth muscle relaxation in (hyperglycemic) saphenous arteries implies that, although the endothelial arginine pool cannot be sufficiently repleted by surrounding smooth muscle cells, this pool is not sufficiently reduced to limit NOS activity in diabetic Arg1-KO^Tie2mice.

EDH-related arterial relaxing responses were reduced in diabetic mice, as shown earlier (Chennupati et al. 2014;

Morikawa et al. 2005),. In mouse mesenteric arteries, endothelium-derived H2O2 mediates these responses (Matoba et al. 2000). The main sources of H2O2 are superoxide dismutases (SODs) (Morikawa et al. 2003).

The superoxide anion substrates of these SODs can be generated by a broad variety of enzymes such as the mito- chondrial electron transfer chain, NADPH oxidases, xan- thine oxidase, cyclooxygenases, lipoxygenase, and NO synthases (Fleming et al. 2001; Katusic 1996; Stroes et al.

1998). Superoxide anion production by NOS (EDH/H2O2

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production by the endothelium) is markedly enhanced by

“uncoupling” and de-dimerization of the enzyme in response to shortage the co-factor BH4 or the substrate (L-Arg) (Munzel et al. 2005; Forstermann and Munzel 2006). Although we did not investigate the underlying mechanism for reduced EDH responses in mouse saphenous arteries during diabetes, substrate availability can be one of the factors. Accordingly, we expected that EDH- dependent relaxation responses in Arg1-KO^Tie2 mice would be reduced. However, this was not observed. Other factors in superoxide/H2O2 generation may have con- tributed.

Diabetic mice displayed reduced smooth muscle sensitivity to exogenous NO. Despite comparable overall endothelium-dependent relaxation, this was more pronounced in Arg1-KO^Tie2 than control mice.

This may indicate increased EDNO production in Arg1-KO^Tie2 mice, which would be in line with our initial hypothesis that substrate abundance in endothelial cells increases NO production. Over time, this could have been compensated by a progressively reduced sensitivity of the arterial smooth muscle cells to NO.

In conclusion, deletion of Arg1 using the Tie2 pro- moter did not affect MAP or heart rate in control mice.

In addition, ex vivo studies of saphenous arteries from control and diabetic mice showed that arterial smooth muscle and endothelium-dependent relaxing responses were largely unaffected by ablation of Arg1 in the endothelium and hematopoietic cells. Comparison of the responses of endothelial Ass (our previous study) and Arg1 ablation may suggest that only ASS-generated arginine is accessible to NOS3 in this model (Flam et al.

2001).

Data availability statement

All data generated or analyzed during this study are included in this published article (and its Supplementary Information files).

Conflicts of interests

The authors declare that there are no conflicts of interest, financial or otherwise.

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Supporting Information

Additional Supporting Information may be found online in the supporting information tab for this article:

Table S1. Fasting blood glucose concentrations in male and female control and Arg1-KO^Tie2 mice before (basal value) and at the indicated times after streptozotocin treatment. All values are shown as means SEM.

Table S2. Effect of Arg1-ablation on saphenous artery (SA) diameter and SA contractile responses in male mice.

E_max values are expressed as % of the maximal response to noradrenaline (10 µmolL ¹NA).

Table S3. P-values of comparisons of plasma amino acid concentrations between control and Arg1-KO^Tie2 mice, and normoglycemic and diabetic mice, respectively.

Table S4.P-values of comparisons of relaxation responses as shown in Table 2.

Table S5. Effect of Arg1-ablation on saphenous artery (SA) diameter, contractile, and relaxation responses in female mice.

Figure S1. Specificity of arginase-1 antibody was demonstrated by simultaneous staining of liver tissue.

Figure S2. The effect of endothelial Arg1 ablation on relaxation responses to ACh (0.01–10 µmolL^–1) during K⁺- (40 mmolL^–1) induced contractions in saphenous arteries of 12- (panel A), 34- (panel B) week-old normoglycemic and 22-week-old diabetic (panel C) male mice.

Black squares: control mice; white circles: Arg1-KO^Tie2 mice.